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Chapter 9 Alcohols, Ethers, and Epoxides
Chapter 9 Alcohols, Ethers, and Epoxides

... • Primary and 2° alcohols can be converted to alkyl halides using SOCl2 and PBr3. • SOCl2 (thionyl chloride) converts alcohols into alkyl chlorides. • PBr3 (phosphorus tribromide) converts alcohols into alkyl bromides. • Both reagents convert ¯OH into a good leaving group in situ—that is, directly i ...
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... If the nitrogen atom is bonded to three carbons it is a tertiary amine. If the nitrogen is bonded to two carbons it is a secondary amine and if the nitrogen is bonded to only one carbon it is a primary amine. ...
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CHM_221_201620 - Oakton Community College
CHM_221_201620 - Oakton Community College

... 1. Apply the three models of bonding–Lewis, valence bond and molecular orbital theory–as well as their extensions–hybridization and resonance–to describe covalent bonding in organic species. 2. Draw and interconvert drawings of neutral and charged organic species using condensed formulae, bond-line ...
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... In a sample of cis-1,2-dimethylcyclohexane at room temperature, the methyl groups will: A) Both be equatorial whenever the molecule is in the chair conformation. B) Both be axial whenever the molecule is in the chair conformation. C) Alternate between both equatorial and both axial whenever the mole ...
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... alkyl group is named as a hydrocarbon chain, and the other is named as part of a substituent bonded to that chain: Name the simpler alkyl group as an alkoxy substituent by changing the –yl ending of the alkyl group to –oxy. Name the remaining alkyl group as an alkane, with the alkoxy group as a subs ...
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... o The alkanes are a subset of the set of hydrocarbons. o The general formula for the alkanes is CnH2n+2. o An alkane can be identified from the ‘-ane’ ending. o Straight-chain alkanes can be named from molecular formulae, shortened and full structural formulae (only C1 to C8). ...
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Group 2 - UC Davis Canvas
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... 11. The bond energy of the noble gas fluorine is too small to offset the energy required to break the F—F bond. 13. Iodide ion is slowly oxidized to iodine, which is yellow-brown in aqueous solution, by oxygen in the air: 4 I − ( aq ) + O 2 ( g ) + 4 H + ( aq )  → 2 I 2 ( aq ) + 2 H 2 O(l) . 15. D ...
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aldehyde ketone

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Alkene



In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond. Alkene, olefin, and olefine are used often interchangeably (see nomenclature section below). Acyclic alkenes, with only one double bond and no other functional groups, known as mono-enes, form a homologous series of hydrocarbons with the general formula CnH2n. Alkenes have two hydrogen atoms less than the corresponding alkane (with the same number of carbon atoms). The simplest alkene, ethylene (C2H4), which has the International Union of Pure and Applied Chemistry (IUPAC) name ethene is the organic compound produced on the largest scale industrially. Aromatic compounds are often drawn as cyclic alkenes, but their structure and properties are different and they are not considered to be alkenes.
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